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Radionuclides and Heavy Metals in the Environment
Dharmendra K. Gupta
Soumya Chatterjee
Clemens Walther Editors
Lead in
Plants and the
Environment
Radionuclides and Heavy Metals
in the Environment
Series Editors:
Dharmendra K. Gupta
Ministry of Environment, Forest and Climate Change
Indira Paryavaran Bhavan, Jorbagh Road
Aliganj, New Delhi, India
Clemens Walther
Gottfried Wilhelm Leibniz Universität Hannover
Institut für Radioökologie und Strahlenschutz (IRS)
Hannover, Germany
More information about this series at http://www.springer.com/series/16207
Dharmendra K. Gupta • Soumya Chatterjee
Clemens Walther
Editors
Clemens Walther
Gottfried Wilhelm Leibniz Universität
Hannover
Institut für Radioökologie und
Strahlenschutz (IRS)
Hannover, Germany
This Springer imprint is published by the registered company Springer Nature Switzerland AG
The registered company address is: Gewerbestrasse 11, 6330 Cham, Switzerland
Preface
Lead (Pb) is a metal utilized by humans for many thousands of years. Metallic Pb
globules manufactured in 6400 BC were discovered at Çatalhöyük (presently in
Republic of Turkey). Pb is a bluish-white lustrous metal, which is very soft, highly
malleable, and ductile, and is a relatively poor electric conductor. Metal is resistant
to corrosion but tarnishes upon exposure to air. In nature, it is typically found as
minerals, in combination with other elements.
A total of 49 isotopes of Pb were recorded till date with four stable isotopes
(204,206,207,208 Pb). Among the stable isotopes, only 204Pb is a primordial nuclide, and
not a radiogenic one. The three other stable isotopes, 206,207,208Pb, are the endpoints
of three decay chains, i.e., uranium, actinium, and thorium series, respectively. 205Pb
and 202Pb are the longest-lived radioisotopes with a half-life of approximately
15.3 million years and 53,000 years, respectively. The radiologically most relevant
radioactive nuclide 210Pb is part of the 238U series and has a half-life of 22.3 years.
210
Pb is suitable for studying the chronology of sedimentation on time scales shorter
than 100 years. Anthropogenic activities, like combustion of coal, are one of the
major sources of 210Pb in the atmosphere, but 210Pb also occurs naturally since it is a
progeny of the radioactive noble gas radon (222Rn) emanating from soil air due to the
omnipresent uranium.
Pb is a microelement with no known physiological function but found in trace
amounts in all biotic resources, e.g., in soil, water, plants, and animals. Pb is a toxic
element, pollution of which may come from various sources. In the environment,
nearly 98% of stable Pb originates from paints, petrochemicals, pipes and supply
systems, etc. Routes of Pb poisoning may be through consumption of contaminated
food and water, breathing contaminated air from cigars and automobile exhausts,
and using uncleaned adulterated hands/face where individual health and hygiene
issues are compromised. However, usually, Pb is not absorbed through skin.
Recent extensive work on 210Pb radioisotope for examining plant uptake, where,
mostly, artificial spiking of the metal in the soil and observing its consequent absorp-
tion in plant and soils. Usually, Pb forms complexes with soil particles, and a very
small amount or fractions are easily available for plants. Despite its lack of essential
function in plants, Pb is taken up mostly through the roots from soil solutions at
v
vi Preface
rhizosphere level, which may cause the entry of Pb into the food chain. It is also
reported that uptake of Pb by roots occurs mainly through apoplastic pathway or via
Ca2+ absorbent channels. Pb in soil and its uptake by plants depends on several fac-
tors, like soil pH, soil particle size, soil moisture, cation-exchange capacity, presence
of other (in)organic substances (including humus), root structure and rhizosphere,
root exudates, and root mycorrhizal properties. Once Pb enters into the plants
through root, initially, it is getting deposited at root cells. However, reports also sug-
gest that negatively charged root cell walls adsorb Pb. Accumulation of Pb in plants
renders phytotoxic symptoms, disturbing morphological, physiological, and bio-
chemical functions, like inhibition of ATP production, lipid peroxidation, and DNA
damage by overproduction of reactive oxygen species (ROS). However, monitoring
Pb remobilization and related secondary pollution and effective, environment-
friendly remediation measures to reduce Pb pollution is the need of the hour.
The main features of this volume are interrelated to how Pb enters into the envi-
ronment and its translocation from soil to plants and into the food chain. Chapters
1 and 2 deal with the analytical methods for determining Pb both in environmental
and in biological samples and also the effect of radioisotopic lead behavior in plants
and environment and distribution of radioactive Pb and its distribution in environ-
ment through modelling application. Chapters 3 and 4 focus on Pb exposure to
humans via agroecosystem and its consequences. Chapters 5 and 6 focus on how Pb
behaves in soil plant system and how it uptakes in plants. Chapters 7 and 8 empha-
size on how Pb reacts on physiological and biochemical changes in plants with
reference to different plant enzymes and photosynthetic apparatus. Last but not
least, Chaps. 9 and 10 present the biological strategies of lichens symbionts, under
Pb toxicity, and how Pb pollution is going to remediate via phytoremediation. The
material composed in this volume will bring in-depth holistic information on Pb
(both stable and radioactive) uptake and translocation and its toxicity in plants and
effect on human health and phytoremediation strategies.
Drs. Dharmendra K. Gupta, Soumya Chatterjee, and Prof. Clemens Walther indi-
vidually acknowledge all authors for contributing their valuable time, information,
and interest to bring this book into its current form.
vii
viii Contents
ix
Major Analytical Methods for Determining
Lead in Environmental and Biological
Samples
Jozef Sabol
Abstract Lead (Pb) is an element which is found in nature where out of its known
49 isotopes the most abundant are four: 208Pb (52%), 206Pb (24%), 207Pb (22%) and
204
Pb (less than 2%). The increased concentration of lead in the environment is
mainly due to some human activities. This includes use of petrol in transport vehi-
cles and releases from industrial and other installations and facilities. From the con-
taminated environment where soil, water, air, animals and plants always contain
certain concentration of lead, the nuclide can find a way into the human organism
by inhalation and ingestion. This results in some health effects which, in the case of
higher intake, may be extremely poisoning and dangerous. Chronic lead intoxica-
tion has been linked to Alzheimer’s disease. Lead, like many heavy elements, tends
to accumulate in bone. Therefore, analysis of the lead presence in environmental
and biological samples is an important prevention measure against harmful conse-
quences which must be minimised and in accordance with the set standards and
limits. The chapter deals with some specific methods recommended for determining
lead in various samples. Special attention is paid to the description of XRF and
PIXE methods and especially methods based on atomic spectroscopy, namely
absorption and emission spectroscopy as well as atomic fluorescence methods.
While the first two methods are essentially considered as non-destructive, the atomic
spectroscopy method falls into the category of destructive methods.
J. Sabol (*)
Department of Crisis Management, Faculty of Security Management, PACR,
Prague, Czech Republic
e-mail: sabol@polac.cz
1 Introduction
Lead (Pb) is a blue-gray malleable metal found in Group 14 (IV A) periodic table of
elements. Natural lead is a mixture of predominantly four stable isotopes: 208Pb,
206
Pb, 207Pb and 204Pb. Altogether, there are 49 known lead isotopes, the occurrences
of the four of them mentioned above are most abundant: 208Pb (52%), 206Pb (24%),
207
Pb (22%) and 204Pb (less than 2%). Of these four isotopes of lead, the only 204Pb
is non-radiogenic (it is not the product of radioactive decay, it originates outside the
decaying series) and its presence on Earth is on Earth is unvarying. The other three
are radiogenic final isotopes of the disintegration series: 206Pb is the final disintegra-
tion product of 238U (uranium 238U decay chain), 207Pb is the final product of 235U
(uranium 235U decay chain), and 208Pb is the ending product of 232Th (Table 1). It is
possible to distinguish with different isotopic composition whether it is a natural or
anthropogenic source. This is possible if all pollution sources are characterised by
their ratio of lead isotopes and pollutants therefore have their own specific isotopic
composition. For example, lead released during combustion processes shows a dif-
ferent isotopic composition of 206Pb/207Pb from other sources of pollution. Also, the
isotopic composition of lead emitted into the atmosphere in metallurgical processes
corresponds to the isotopic composition of the original materials.
Lead was known and used since prehistoric times. Exposure to lead has been
consequently increased mainly because the environment is more and more contami-
nated by this element. Although acute lead poisoning has become sporadic, chronic
exposure to low levels of lead is still considered to be a public health issue (Shilu
et al. 2000). Lead intake can lead to a variety of adverse health impacts All over the
word; the relevant standards for lead emissions have become increasingly stringent
because of new findings about its possible health impacts. The associated regula-
tions require monitoring the situation in order to keep the level and lead concentra-
tion below the limits and action levels set by national regulatory authorities.
Lead had previously been mainly introduced into the waters by road and vegeta-
tion flushes from the immediate vicinity of busy roads. The exhaust gas contained
lead as the decomposition products of tetra-alkyl, which was a common anti-knock
additive for gasoline. To a lesser degree lead and lead alloy plants also contribute to
contamination. It also gets into the water from the lead pipe. The tetra-alkyl com-
pounds are very volatile and easily pass into the atmosphere when aerating the water.
It accumulates in bones and other tissues with age. It interferes with red blood cell
enzymes and may cause death at higher doses, causing mental retardation. Often
enough lead (200 mg kg−1) in the grass along the highways could even kill cattle.
The nuclides produced as results of the decay of natural radionuclides with very
long half-life such as 238U (half-life 4.5 109 years), 235U (half-life 0.7 109 years) and
232
Th (half-life 14 109 years) are radioactive and continue to form more radioactive
nuclides until a non-radioactive nuclide is formed. A uranium-radium decay chain
begins with 238U and ends with the stable 206Pb after going through 18 intermediate
steps. Uranium-235 is at the beginning of the uranium-actinium decay chain leading
via 15 radionuclides to 207Pb. With ten intermediate states, the thorium decay chain
Major Analytical Methods for Determining Lead in Environmental and Biological… 3
Table 1 Three main decay chains (or families) are observed in nature, commonly called the
thorium series, the radium or uranium series, and the actinium series, representing three of these
four classes, and ending in three different, stable isotopes of lead (A, mass number corresponding
to number of protons and neutrons; Z atomic or proton number; N number of neutrons)
(continued)
4 J. Sabol
Table 1 (continued)
starting with 232Th and ending at 208Pb is the shortest. The daughter nuclides arising
from the disintegration of naturally occurring 238U, 235U and 232Th are all radioactive
and therefore disintegrate until the last one which is stable lead, namely 206Pb, 207Pb
and 208Pb, respectively.
2 Health Effects
While the use of lead has been greatly reduced in developed countries, it is still used
widely in developing countries because it has some unique useful properties suit-
able and required in a number of various applications. The continued use of lead has
caused its levels to raise worldwide, posing serious threats not only to the environ-
ment but also to the humans living in it. Lead can cause some damage in every organ
and tissue in human body, Exposure to high lead levels can severely affect the brain
and kidneys and eventually cause death. High levels of exposure can lead to miscar-
riage in pregnant women. Lead is also widely thought to be cancerogenic. Toxic
effects of lead have been observed especially on the renal, reproductive and nervous
system. Therefore, some the techniques were developed for treating lead toxicity.
Some more information about the recent progress in this area is given in the review
Major Analytical Methods for Determining Lead in Environmental and Biological… 5
(Wani et al. 2015). An overview of possible health effects caused by lead which
entered human body through various routes is given in Table 2.
In general, it has been widely accepted that lead is a probable human carcinogen.
Lead can affect every organ and system in the body. Exposure to high lead levels can
severely damage the brain and kidneys and ultimately cause death. In pregnant
women, high levels of exposure to lead may cause miscarriage. Internationally for
lead regulatory limits have been introduced corresponding to15 parts per billion
(ppb) in drinking water and 0.15 μg per cubic meter in air.
Since lead is an element that occurs naturally in the earth, trace amounts of lead
may occur in the foods we eat and the water we drink. Regulatory authorities in
most countries are trying to control population exposure to lead from various
sources. The main sources of lead entering human body include the following:
• Inhalation of lead dust which originates from lead-based paint and lead-
contaminated soil.
• Touching by hands other objects contaminated with lead dust and then putting
them into mouths.
• Consuming food, candy or water contaminated by lead.
• By means of dishes or glasses that contain lead.
• From colour additives in paints and cosmetics (special case may be children
playing with toys that contain lead paint).
In addition to occupationally related exposure by some workers, the most sensi-
tive group among population represent children, which may be affected by lead due
to many different situations (Fig. 1).
6 J. Sabol
There are several methods used for the monitoring and identification of the occur-
rence of lead in analysed samples. The techniques differ as to sample preparation
and treatment as well as to instrumentation used.
The principles of both methods are similar. In case of X-ray fluorescence (XRF)
method, an incident X-ray photon removes an orbital electron leaving a hole which
is filled by an electron from an outer shell which results in the emission of a photo-
electron and a characteristic photon with an energy inherent to the type of the atom
of a nuclide under examination. The PIXE (particle induced X-ray emission) method
is essentially the same, only instead incident X-ray photons charge particles (in
most cases protons) are used. The process is illustrated in Fig. 2.
X-ray photons or charged particles excite inner electron shells of the sample
material. The ejected electron leaves the atom of the target element as a photoelec-
tron. Other electrons fill the gap and give off large amounts of energy in the form of
characteristic X-rays, which are detected, their energy can thus identify the element,
and the intensity of X-rays identifies concentration of the element in the sample. In
general, incident photons may be produced either by an X-ray tube or a radionuclide
emitting soft gamma radiation.
As a source of primary radiation, the XRF analysers can use either an X-ray tube
(Fig. 3a) or a suitable radioactive excitation source (Fig. 3b) such as 57Co and 109Cd.
In addition to laboratory XRF analysers, usually equipped with radioactive
sources, there are several various types of portable analysers (Fig. 4) designed to
Major Analytical Methods for Determining Lead in Environmental and Biological… 7
Fig. 2 The principle of the mechanism of XRF (and PIXE) method; (a) the generation of charac-
teristic photons; (b) their energy distribution (Based on Motohiro et al. 2015)
Fig. 3 Basic arrangement of an XRF analyser using (a) an X-ray tube and (b) a radioactive source
monitor the detection of heavy metals (including Pb) in soil, paint, toys, and so on.
These handheld XRF analysers can also be used for specific material identification
and hazardous material analysis, and for metal alloy identification, consumer goods
screening, compliance screening and many other analysis needs. These analysers
serve also for checking compliance with the standards and limits introduced by the
relevant regulatory authorities,
An X-ray spectrographic technique known as the PIXE method, can be used to
analyse solid, liquid or aerosol filter samples in a non-destructive, simultaneous
elemental way. The X-ray photons are initiated when energetic protons excite target
atoms in the inner shell of electrons. When these inner shell electrons are subse-
quently expelled, they produce X-rays whose energies are emitted when the result-
ing vacancies are again filled. These vacancies are unique to the sample elements
being analysed, with the number of X-rays emitted being proportional to the mass
of the corresponding sample element.
8 J. Sabol
Fig. 4 Some examples of portable XRF analysers, (a) Oxford X-MET5000 Handheld XRF
Analyzer (Oxford 2019) and (b) Thermo scientific XRF analyser (Thermo 2019)
The PIXE method for the most part uses protons to generate X-rays in a sample,
the probability of which depends on the proton energy (in MeV) as well as on the
total number of incident protons. This number can be expressed as proton current
(in mA): the greater the proton current, the greater the probability for X-ray
production. As the proton energy changes, the probability for X-ray production also
changes. Both of these factors must be accurately known in order to perform a cor-
rect quantitative analysis. When protons interact to produce X-rays, each collision
in turn transfers kinetic energy from the mobile proton to the immobile target atom.
While each collision produces a small amount of energy, as the collisions and result-
ing energy increase, they eventually reduce the proton’s energy as well as its ability
to generate X-rays, and in the end the proton becomes immobile. The instrument
calibration is carried out at specific proton energy, Data on proton energy loss is
necessary to calibrate instruments for performing accurate quantitative analysis.
Since instrument calibration is carried out at specific proton energy, information of
the proton energy loss is indispensable for quantitative analysis. The PIXE tech-
nique has been used in the monitoring of lead and other metals. The range of Pb
concentrations in human rib bone was found to be in the range of 1.4–11.5 μg g-1 for
the trabecular surface by PIXE (Deibel et al. 1995).
Fig. 5 The illustration of all three techniques of atomic spectroscopy based on atomic emission,
atomic absorption and atomic fluorescence
−( k . n . l )
I = I0e
where I0 is the intensity of the exciting radiation, I is the intensity of the radiation
after passing through the absorbing environment (flame), k is the atomic absorption
coefficient for the specified absorption line, n is the number of atoms of the analysed
element in the volume unit and l is the length of the absorption layer.
In practice, the logarithm of the attenuation of light energy called absorbance (A)
is used as the measure corresponding to the concentration of the nuclide monitored.
The absorbance is expressed by the relation
I0
A = log = 2.303 ( k.n.l )
I
A very simple linear dependence on the atomic concentration of the measured ele-
ment is then valid for absorbance. Therefore, all AAS spectrometers indicate the mea-
sured results in terms of absorbance units reflecting the actual measured light transmittance.
Individual parts of a common atomic absorption spectrometer are shown in Fig. 6.
The atomic emission spectrometry is suitable for the assessment of lead concen-
tration in various waters. Results of some measurements in Iran are presented in
Table 3 (Dadfarnia et al. 2001). Another table (Table 4) illustrates the use of atomic
absorption spectrometry in determining lead concentration in tea leaves, mixed
Polish herbs and oriental tobacco leaves (Chwastowska et al. 2008). The same
authors (Chwastowska et al. 2008) measured also lead concentration in soil, street
dust and grass with the results of 67.6, 21.3 and 2.0 μg g−1, respectively.
Major Analytical Methods for Determining Lead in Environmental and Biological… 11
Table 4 Results of analysis of the concentration of lead together with Cu and Cd determined in
three different samples
Sample Pb (μg g−1) Cu (μg g−1) Cd (μg g−1)
Tea leaves 1.78 ± 0.24 20.4 ± 1.5 0.030 ± 0.004
Mixed Polish herbs 2.16 ± 0.23 7.77 ± 0.53 0.199 ± 0.015
Oriental tobacco leaves 4.91 ± 0.80 14.1 ± 0.50 1.12 ± 0.12
Atomic emission spectroscopy relies on the principle that when light or heat is
applied to a molecule, it gets excited and moves to a higher energy level, making it
unstable. The excited molecule then jumps to a lower energy level, thereby emitting
photons of characteristic energy. The emitted wavelengths are then recorded in the
emission spectrometer.
Similarly, to atomic absorption spectroscopy, the sample should be transformed into
free atoms. This is normally achieved using a high-temperature excitation source.
Liquid samples are dispersed and led in the excitation source by a flowing gas. Solid
samples can be introduced into the source by slurry or by laser ablation of the solid
sample in a gas stream. Solids can also be directly vaporised and excited by a spark
between electrodes or by a laser pulse. The excitation source must desolvate, atomise,
and excite the analyte atoms. The excitation sources include flame, inductively coupled
plasma, laser-induced plasma, direct-current plasma, microwave-induced plasma and
spark or arc. The basic scheme of a standard atomic emission spectrometer is in Fig. 7.
12 J. Sabol
Fig. 7 Principal
arrangement of an atomic
emission spectrometer
An X-ray region in the electromagnetic spectrum is that which lies between the wave-
lengths of 0.01 and 10 nm. X-rays are produced, for example, in elementary reactions
particles, in the decay of radioactive elements and other processes. Secondary X-rays
are also produced by exposing the sample with appropriate (primary) X-rays. This
phenomenon is called X-ray fluorescence and is the basis for qualitative and quantita-
tive X-ray fluorescence spectroscopy (XRF—X-ray fluorescence) analytical tech-
niques. Upon absorption of the primary photon by the electron in the inner shell of
the atom, the release of this electron (photo effect) and the formation of an electron
hole occur. This hole is filled with an electron jumping from higher energy level. In
doing so, the secondary (fluorescent) X-rays are released, the spectrum of which is of
a line character and characteristic of the element being analysed.
As a source of the fluorescent radiation, usually an X-ray tube or suitable radio-
active sources are used. The X-ray source consists of an evacuated tube, tungsten
fibre cathode, water-cooled target anode (Ca, Rh, Pd, Ag, W), supplied voltage
source (5–80 kV) and a beryllium window. A radioactive source is an appropriate
radionuclide emitting gamma radiation which is usually of lower intensity com-
pared to X-ray tube. These sources are especially useful in smaller and portable
spectrometers. Characteristic parameters of some suitable radionuclides used in
XRF spectrometers are presented in Table 5.
4 Conclusion
Lead is clearly among the toxic elements. Historically, overuse of lead is one of the
factors that have contributed to the extinction of the Roman Empire. The main con-
tribution to the excessive intake of lead was due to the use of lead acetate as a sweet-
ener. At present, lead is a ubiquitous environmental contaminant due to the use of
lead in drinking water installations, in the production of paints, as an additive in
gasoline and its other industrial applications. Lead penetrates into the body mainly
in the bone, and a certain amount is found in the blood. Even traces of lead in the
environment and food can lead to subsequent severe illnesses, as lead is accumulated
in the body. Therefore, the instrumentation for the measurement and monitoring of
Major Analytical Methods for Determining Lead in Environmental and Biological… 13
References
Fatih Külahcı
Abstract The abundance of lead element with an atomic number 82 is 1.03 × 10−8
% in the Solar System, 14 mg kg−1 in the Earth’s surface and 3 × 10−5 mg L−1 in the
oceans. The most dangerous radioisotope of lead is the 210Pb, which has a half-life
of 22.26 years and gamma energy of 46.5 keV. Modelling is one of the most effec-
tive ways of appreciation about the distribution effects and transport of the elements
to the earth. It has a wide range of content from pure differential equations to spatial
analysis calculations. In this section, the modelling with Monte Carlo Simulation
method of the environmental distribution of the lead can be found. The Monte Carlo
Simulation method on 210Pb data lead to concentrations for future times. In addition,
models of auto regressive integrated average (ARIMA), generalized autoregressive
conditional heteroscedastic (GARCH) and autoregressive conditional heteroscedas-
tic (ARCH) are obtained to determine the environmental distribution characteristics
of the lead. The proposed simulation methodologies can also be used successfully
for other variables other than lead.
1 Introduction
Lead (Pb) is one of the most important pollutants and its mining, production and
recovery are possible in the environment its use in technology, and especially, in
shielding, battery and toy industry. Pb is available in a high proportion within the
F. Külahcı (*)
Science Faculty, Physics Department, Nuclear Physics Division, Firat University,
Elazig, Turkey
e-mail: fatihkulahci@firat.edu.tr
earth’s crust (Table 1) and is spread to the atmosphere and environment by dust
storms, volcanic movements and water passing through the rocks.
In this section the focus is on the radioactive 210Pb, which is difficult to study
chemically and physically, depending on the relatively low radioactive energy. Pb
has 49 radioisotopes of which only three are stable (Table 2).
2 Radioactive Lead
Naturally occurring radioactive lead nuclei have 214Pb (t1/2 = 26.8 min) from 238U,
210
Pb (t1/2 = 22.3 years) from 238U, 211Pb (t1/2 = 36.1 min) from 235U, and 212Pb
(t1/2 = 10.64 h) from 232Th. Due to its relatively long half-life, 210Pb is the most
remarkable among other radioisotopes. Although the half-lives of other radionu-
clides are relatively small in the geological time scale, they are continuously repro-
duced, because they are members of the U and Th disintegration series and degraded
by these core nuclei. Different fractions of radioactive lead are found in significant
amounts in nature (Valkovic 2000). When 210Pb breaks down to decay product 210Bi
(t1/2 = 5.013 days), high energy Bremsstrahlung causes beta radiation, which is a
major problem for detector systems. High-energy beta radiation increases back-
ground radiation, so it is necessary to take care when using lead shields in detectors.
If the detection systems are protected from external background radiation then they
can produce strong Bremsstrahlung radiation, which causes the spectroscopic sys-
tems to take incorrect measurements.
Environmental Distribution and Modelling of Radioactive Lead (210): A Monte Carlo… 17
Table 2 List of lead nuclides (adopted from Kaye 1995; Lide and Frederikse 1995)
Nuclide Half-Life Abundance
Pb-181 45 ms
Pb-182 55 ms
Pb-183 300 ms
Pb-184 0.55 s
Pb-185 4.1 s
Pb-186 4.83 s
Pb-187 18.3 s
Pb-188 24 s
Pb-189 51 s
Pb-190 1.2 m
Pb-191 1.33 m
Pb-192 3.5 m
Pb-193 ~2 m
Pb-194 12.0 m
Pb-195 ~15 m
Pb-196 37 m
Pb-197 8m
Pb-198 2.40 h
Pb-199 90 m
Pb-200 21.5 h
Pb-201 9.33 h
Pb-202 5.25E4 years
Pb-203 51.873 h
Pb-204 >1.4E17 years 1.400%
Pb-205 1.53E+7 years
Pb-206 Stable 24.100%
Pb-207 Stable 22.100%
Pb-208 Stable 52.400%
Pb-209 3.253 h
Pb-210 22.3 years
Pb-211 36.1 m
Pb-212 10.64 h
Pb-213 10.2 m
Pb-214 26.8 m
Pb-215 36 s
Pb-187m 15.2 s
Pb-191m 2.18 m
Pb-193m 5.8 m
Pb-195m 15.0 m
Pb-197m 43 m
Pb-199m 12.2 m
Pb-201m 61 s
(continued)
18 F. Külahcı
Table 2 (continued)
Nuclide Half-Life Abundance
Pb-202m 3.53 h
Pb-203m 6.3 s
Pb-204m 67.2 m
Pb-205m 5.54 ms
Pb-207m 0.805 s
Pb-193m2 5.8 m
Pb-203m2 0.48 s
Pb emits 16.96 keV of 84% intensity and 63.50 keV of beta radiation with
210
intensity of 16%. When detecting 210Pb, high-purity Ge detectors detect 46.54 keV
gamma emission energies at the intensity of 4.25%.
3 Modelling of 210Pb
1 n 2
γ ( di ) = ∑ ( CVt ) j − ( CVt ) j −1 (1)
2 j =1
Fig. 2 Simulation curves calculated with STPCSV for Hazar Lake, Turkey. (a) Radius of influ-
ence for 1 km at 1 h; (b) radius of influence for 1 km at 3 h; (c) radius of influence for 1 km at 5 h;
(d) radius of influence for 3 km at 5 h; (e) radius of influence for 3 km at 1 h; (f) radius of influence
for 3 km at 3 h
20 F. Külahcı
Fig. 3 210
Pb histogram plot
−( x − µ )
2
1
y = f ( x µ ,σ ) = e 2σ 2
(2)
σ 2π
SPRINGING FORWARD HE
CAUGHT THE CLUB.
For the present, my pen is here laid aside. I shall wait to see what
use the Lord makes of Part First of my autobiography, before I
prosecute the theme. If the Christian public seems not to find in it
the help and quickening that some friends think it likely to bestow on
those who read, the remainder need not be written. Part Second, if
called for, will contain a record, in many respects, an utter contrast
to all that has gone before, and yet directly springing therefrom, as
will be seen by all who look beneath the surface. I am penning these
words in 1887, and five-and-twenty years lie betwixt this date and
my farewell to Tanna. These years, if ever published, will tell the
story of my visiting all the Colonial Churches, and collecting the
purchase money of our white-winged Mission Ship, the Dayspring;
my return to Scotland, visiting all the home congregations in 1864,
and securing several new Missionaries to follow me to the New
Hebrides; my second marriage, and settlement on Aniwa, with her
whom the good Lord still spares to me, the mother of our happy
family, and my God-given helpmeet in all the work of the Gospel; the
conversion of that whole island of Aniwa from idolatry, and the
planting there of a Church and Congregation of Christ, from which
have since gone forth many Native Evangelists and Teachers. Then
there will fall to be recorded my call from the Islands in recent years
to revisit all the Colonial Presbyterian Congregations once again,
telling them the story of the Conversion of Aniwa—the sinking of the
well, and other incidents, which turned an entire people from idols
and from cannibalism to the service of the living and true God—
whereby the Churches, and especially the children, were led more
and more to make the New Hebrides their own very harvest field in
the Heathen world. And finally, I will have to tell how I was again
sent home to Scotland in 1884 to raise money for the purchase or
building of a steam-auxiliary Mission Ship, now urgently required in
the interests of the Mission, both because of the great increase in the
number of the Missionaries and the necessities of so many families;
and also and chiefly to avert the dreadful disappointments and loss
of time, and thereby sometimes of life itself, caused by the frequent
becalming of our little Dayspring in these thickly-islanded seas. That
part of the story will show the fruits of the education and perils and
experiences of a lifetime, in the marvellous impression produced by
the simple and unadorned recital of the story of Tanna and Aniwa,
amongst the Christian people of Scotland, Ireland, and England.
Multitudes were blessed in almost every town where a meeting was
granted me. Three Missionaries devoted themselves to the New
Hebrides, and are already labouring there; while others consecrated
themselves to several of the great seats of Foreign Mission enterprise
in Africa and Asia. I returned to my own Church of Victoria with a
sum of nearly £9,000, of which £6,000 was for the new Missionary
Steam-Auxiliary, and the remainder for the outfit and support of
more Missionaries for the Islands; and that money I handed over to
the Australian Church, where it awaits, at interest in the bank, the
arrangements being made by all the Colonies to take each their due
share in the future up-keep of the Ship. For this—for everything—for
all, praise be to the Lord! I never asked one subscription, except in
prayer and in my public appeals. The Lord sent in all freely to me
through the hands of His people; to Him be all the glory. I went back
to Aniwa, and found the work of the Lord going forward there as if in
a regularly settled Congregation at home, fostered and guided by an
occasional visit of my ever dear and genuine friends, Mr. and Mrs.